Verification Results Template (Change Control)

Description

This verification results template contains all the information you need to get started recording the verification of the correct implementation of an action plan to address changes. We designed it for companies that need to comply with:

• ISO 13485,
• EU Medical Device Regulations 2017/745, and
• FDA 21 CFR 820.

This template includes detailed information about how to fill out each section.
It is designed to be used with the company’s own change control procedure, or with a compatible change control procedure from this site.

The verification results is crucial to evaluate the effectiveness of the a change’s action plan implementation. The verification results is based on the verification protocol outlined in the action plan.

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